Canonical Allele Identifier: CA2483126542

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770806_206770808delinsCTG , CM000663.2:g.206770806_206770808delinsCTG	GRCh38
NC_000001.10:g.206944151_206944153delinsCTG , CM000663.1:g.206944151_206944153delinsCTG	GRCh37
NC_000001.9:g.205010774_205010776delinsCTG	NCBI36
NG_012088.1:g.6687_6689delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+99_283+101delinsCAG (IL10)
ENST00000471071.2:c.123+99_123+101delinsCAG (IL10)	ENSP00000493073.2:n.123+99_123+101delinsCAG
ENST00000659065.2:c.261+99_261+101delinsCAG (IL10)	ENSP00000499588.1:n.261+99_261+101delinsCAG
ENST00000659642.2:c.261+99_261+101delinsCAG (IL10)	ENSP00000499509.1:n.261+99_261+101delinsCAG
ENST00000664374.2:c.261+99_261+101delinsCAG (IL10)	ENSP00000499664.1:n.261+99_261+101delinsCAG
ENST00000659997.3:c.-421_-419delinsCTG (IL19) MANE Select	ENSP00000499459.2:n.-421_-419delinsCTG
ENST00000656872.2:c.-173_-171delinsCTG (IL19)	ENSP00000499487.2:n.-173_-171delinsCTG
ENST00000659065.1:c.261+99_261+101delinsCAG (IL10)	ENSP00000499588.1:n.261+99_261+101delinsCAG
ENST00000659642.1:c.261+99_261+101delinsCAG (IL10)	ENSP00000499509.1:n.261+99_261+101delinsCAG
ENST00000659997.2:c.-421_-419delinsCTG (IL19)	ENSP00000499459.2:n.-421_-419delinsCTG
ENST00000662320.1:n.43_45delinsCTG (IL19)
ENST00000664374.1:c.261+99_261+101delinsCAG (IL10)	ENSP00000499664.1:n.261+99_261+101delinsCAG
ENST00000367099.3:n.283+99_283+101delinsCAG (IL10)
ENST00000423557.1:c.378+99_378+101delinsCAG (IL10) MANE Select	ENSP00000412237.1:n.378+99_378+101delinsCAG
ENST00000471071.1:n.293+99_293+101delinsCAG (IL10)
NM_000572.2:c.378+99_378+101delinsCAG (IL10)	NP_000563.1:n.378+99_378+101delinsCAG
XM_011509506.1:c.378+99_378+101delinsCAG (IL10)	XP_011507808.1:n.378+99_378+101delinsCAG
NM_000572.3:c.378+99_378+101delinsCAG (IL10) MANE Select	NP_000563.1:n.378+99_378+101delinsCAG
NM_153758.3:c.-307_-305delinsCTG (IL19)	NP_715639.1:n.-307_-305delinsCTG
NM_001382624.1:c.123+99_123+101delinsCAG (IL10)	NP_001369553.1:n.123+99_123+101delinsCAG
NM_001393490.1:c.-173_-171delinsCTG (IL19)	NP_001380419.1:n.-173_-171delinsCTG
NM_153758.5:c.-421_-419delinsCTG (IL19) MANE Select	NP_715639.2:n.-421_-419delinsCTG
NR_168466.1:n.437+99_437+101delinsCAG (IL10)